CLINICAL CORRELATIONS AND MOLECULAR ANALYSIS OF HUMAN CYTOMEGALOVIRUS (HCMV) INFECTION IN BRAZILIAN PATIENTS WITH SICKLE CELL DISEASE, BETA-THALASSEMIA MAJOR, AND BLOOD DONORS

被引:0
|
作者
Nanev Slavov, S. [1 ]
Kashima, S. [1 ]
de Deus Wagatsuma, V. [1 ]
Silva-Pinto, A. [1 ]
Covas, D. [2 ]
机构
[1] Hemoctr Ribierao, Ribeirao Preto, Brazil
[2] Fac Med Ribeirao Preto, Dept Clin Med, Ribeirao Preto, Brazil
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
P430
引用
收藏
页码:182 / 182
页数:1
相关论文
共 50 条
  • [21] Microarray analysis of liver gene expression in iron overloaded patients with sickle cell anemia and beta-thalassemia
    Flanagan, Jonathan M.
    Steward, Shirley
    Hankins, Jane S.
    Howard, Thad M.
    Neale, Geoffrey
    Ware, Russell E.
    AMERICAN JOURNAL OF HEMATOLOGY, 2009, 84 (06) : 328 - 334
  • [22] Successful generation of human cytomegalovirus (HCMV)-specific T cell lines from immunodeficient patients with refractory HCMV infection or from HCMV-negative donors
    Basso, S.
    Guido, I.
    Quartuccio, G.
    Gurrado, A.
    Acquafredda, G.
    Rubert, L.
    Compagno, F.
    Del Fante, C.
    Viarengo, G.
    Perotti, C.
    Zecca, M.
    Comoli, P.
    BONE MARROW TRANSPLANTATION, 2017, 52 : S163 - S163
  • [23] CLINICAL AND LABORATORY EFFECTS OF LONG-TERM ADMINISTRATION OF HYDROXYUREA TO PATIENTS WITH SICKLE-CELL/BETA-THALASSEMIA
    VOSKARIDOU, E
    KALOTYCHOU, V
    LOUKOPOULOS, D
    BRITISH JOURNAL OF HAEMATOLOGY, 1995, 89 (03) : 479 - 484
  • [24] Activin-A is elevated in patients with thalassemia major and double heterozygous sickle cell/beta-thalassemia and correlates with markers of hemolysis and bone mineral density
    Ersi Voskaridou
    Ioannis Ntanasis-Stathopoulos
    Dimitrios Christoulas
    Maria Dimopoulou
    Veroniki Komninaka
    Konstantina Repa
    Athanasios Papatheodorou
    Evangelos Terpos
    Annals of Hematology, 2019, 98 : 1583 - 1592
  • [25] Activin-A is elevated in patients with thalassemia major and double heterozygous sickle cell/beta-thalassemia and correlates with markers of hemolysis and bone mineral density
    Voskaridou, Ersi
    Ntanasis-Stathopoulos, Ioannis
    Christoulas, Dimitrios
    Dimopoulou, Maria
    Komninaka, Veroniki
    Repa, Konstantina
    Papatheodorou, Athanasios
    Terpos, Evangelos
    ANNALS OF HEMATOLOGY, 2019, 98 (07) : 1583 - 1592
  • [26] Prevalence of Red Blood Cell Alloimmunization Among Beta-Thalassemia and Sickle Cell Anemia Patients: a Study from Saudi Arabia
    Felimban, Raed
    Alsharyufi, Ahmed
    Aljehani, Jasem
    Sahlool, Ahmed
    Aljabri, Hamead
    Qadah, Talal
    CLINICAL LABORATORY, 2021, 67 (10) : 2323 - 2330
  • [27] Prevalence of hepatitis E virus infection in multiple transfused Brazilian patients with thalassemia and sickle cell disease
    Slavov, Svetoslav N.
    Maconetto, Juliana D. M.
    Martinez, Edson Z.
    Silva-Pinto, Ana Cristina
    Covas, Dimas T.
    Eis-Huebinger, Anna Maria
    Kashima, Simone
    JOURNAL OF MEDICAL VIROLOGY, 2019, 91 (09) : 1693 - 1697
  • [28] PDGF, PDGFR AND TGF GENE EXPRESSION PROFILE IN PATIENTS WITH BETA-THALASSEMIA AND SICKLE CELL DISEASE WITH AND WITHOUT PULMONARY HYPERTENSION
    Polonifi, K.
    Kapellos, G.
    Farmakis, D.
    Aessopos, A.
    Polizos, A.
    Mantzourani, M.
    HAEMATOLOGICA, 2014, 99 : 183 - 184
  • [29] RHCE diversity among Brazilian patients with sickle cell disease (SCD) and selected groups of blood donors
    Arnoni, Carine Prisco
    Vendrame, Tatiane
    Muniz, Janaina
    Cortez, Afonso
    Latini, Flavia
    Castilho, Lilian
    TRANSFUSION, 2021, 61 (12) : 3473 - 3482
  • [30] Human parvovirus 4 in Brazilian patients with haemophilia, beta-thalassaemia major and volunteer blood donors
    Slavov, S. N.
    Kashima, S.
    Rocha-Junior, M. C.
    Silva-Pinto, A. C.
    Oliveira, L. C.
    Eis-Huebinger, A. M.
    Covas, D. T.
    HAEMOPHILIA, 2015, 21 (01) : E86 - E88